Nanoencapsulation strategy is introduced onto a state-of-the-art thermally activated delayed fluorescence (TADF) molecule, i.e. 4CzIPN, which ensures the achievement of air-stable, water-soluble TADF nanoparticles featuring efficient TADF property without unsatisfactory...

Electrochemiluminescence (ECL) based on conjugated polymers or oligomers is persistently being pursued owing to its huge application scope ranging from ultra-sensitive bioanalysis to ultra-resolution imaging and spectroscopy. Because of the theoretical limit in radiative exciton generation yield (typicallỹ 25 %) of those polymers or oligomers, the corresponding ECL efficiency is still limited, which hampers its ECL performance and its related applications. Herein, we report ECL based on a thermally activated delayed fluorescence (TADF) polymer scaffold, which is characteristic of all-exciton harvesting in the ECL process, and thus potentially capable of achieving~100 % ECL efficiency. These desired properties of the TADF polymer ECL is attributed to a fast and efficient up-conversion process from non-radiative triplet to radiative singlet states under thermal activation, which is absent in conventional fluorescent polymers/oligomers, such as F8BT. In this study, various ECL modes, including annihilation or co-reactant mode using TPrA or S 2 O 8 2À as co-reactant, are confirmed for our model TADF polymer ECL system, which was different from fluorescent polymer ECL counterpart. Furthermore, solid-state ECL sensing on L-cysteine (an important marker of disease) is also evaluated by using the model TADF polymer. Ultralow detection limit in combination with high sensitivity and good specificity are achieved for this model system, indicative of a high potential of the TADF polymer scaffold for applications in the broad field of ECL.

An efficient copper‐catalyzed remote C‐5 sulfonylation of 8‐aminoquinoline amides using stable and readily available arylsulfonyl hydrazides has been developed. In the presence of 10 mol‐% Cu(OAc)2 as a catalyst and Ag2CO3 as an oxidant, a wide range of 8‐aminoquinoline amides underwent sulfonylation with arylsulfonyl hydrazides to generate structurally diverse aryl sulfones in moderate to good yields.

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